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Detection of Tuberculosis in HIV-Infected and -Uninfected African Adults Using Whole Blood RNA Expression Signatures: A Case-Control Study
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نویسنده
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kaforou m. ,wright v.j. ,oni t. ,french n. ,anderson s.t. ,bangani n. ,banwell c.m. ,brent a.j. ,crampin a.c. ,dockrell h.m. ,eley b. ,heyderman r.s. ,hibberd m.l. ,kern f. ,langford p.r. ,ling l. ,mendelson m. ,ottenhoff t.h. ,zgambo f. ,wilkinson r.j. ,coin l.j. ,levin m.
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منبع
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plos medicine - 2013 - دوره : 10 - شماره : 10
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چکیده
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Background:a major impediment to tuberculosis control in africa is the difficulty in diagnosing active tuberculosis (tb),particularly in the context of hiv infection. we hypothesized that a unique host blood rna transcriptional signature would distinguish tb from other diseases (od) in hiv-infected and -uninfected patients,and that this could be the basis of a simple diagnostic test.methods and findings:adult case-control cohorts were established in south africa and malawi of hiv-infected or -uninfected individuals consisting of 584 patients with either tb (confirmed by culture of mycobacterium tuberculosis [m.tb] from sputum or tissue sample in a patient under investigation for tb),od (i.e.,tb was considered in the differential diagnosis but then excluded),or healthy individuals with latent tb infection (ltbi). individuals were randomized into training (80%) and test (20%) cohorts. blood transcriptional profiles were assessed and minimal sets of significantly differentially expressed transcripts distinguishing tb from ltbi and od were identified in the training cohort. a 27 transcript signature distinguished tb from ltbi and a 44 transcript signature distinguished tb from od. to evaluate our signatures,we used a novel computational method to calculate a disease risk score (drs) for each patient. the classification based on this score was first evaluated in the test cohort,and then validated in an independent publically available dataset (gse19491).in our test cohort,the drs classified tb from ltbi (sensitivity 95%,95% ci [87-100]; specificity 90%,95% ci [80-97]) and tb from od (sensitivity 93%,95% ci [83-100]; specificity 88%,95% ci [74-97]). in the independent validation cohort,tb patients were distinguished both from ltbi individuals (sensitivity 95%,95% ci [85-100]; specificity 94%,95% ci [84-100]) and od patients (sensitivity 100%,95% ci [100-100]; specificity 96%,95% ci [93-100]).limitations of our study include the use of only culture confirmed tb patients,and the potential that tb may have been misdiagnosed in a small proportion of od patients despite the extensive clinical investigation used to assign each patient to their diagnostic group.conclusions:in our study,blood transcriptional signatures distinguished tb from other conditions prevalent in hiv-infected and -uninfected african adults. our drs,based on these signatures,could be developed as a test for tb suitable for use in hiv endemic countries. further evaluation of the performance of the signatures and drs in prospective populations of patients with symptoms consistent with tb will be needed to define their clinical value under operational conditions.please see later in the article for the editors' summary. © 2013 kaforou et al.
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آدرس
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section of paediatrics and wellcome trust centre for clinical tropical medicine,division of infectious diseases,department of medicine,imperial college london,london,united kingdom,department of genomics of common disease,school of public health,imperial college london,london, United Kingdom, section of paediatrics and wellcome trust centre for clinical tropical medicine,division of infectious diseases,department of medicine,imperial college london,london, United Kingdom, section of paediatrics and wellcome trust centre for clinical tropical medicine,division of infectious diseases,department of medicine,imperial college london,london,united kingdom,clinical infectious diseases research initiative,institute of infectious diseases and molecular medicine,university of cape town,cape town, South Africa, karonga prevention study,chilumba,karonga district,malawi,institute of infection and global health,university of liverpool,liverpool,united kingdom,department of infectious disease epidemiology,london school of hygiene and tropical medicine,london, United Kingdom, brighton and sussex medical school,university of sussex,brighton,united kingdom,university of malawi college of medicine,blantyre, Malawi, clinical infectious diseases research initiative,institute of infectious diseases and molecular medicine,university of cape town,cape town, South Africa, brighton and sussex medical school,university of sussex,brighton,united kingdom,university of malawi college of medicine,blantyre, Malawi, section of paediatrics and wellcome trust centre for clinical tropical medicine,division of infectious diseases,department of medicine,imperial college london,london,united kingdom, karonga prevention study,chilumba,karonga district,malawi,department of infectious disease epidemiology,london school of hygiene and tropical medicine,london, United Kingdom, department of immunology and infection,london school of hygiene and tropical medicine,london, United Kingdom, red cross war memorial children's hospital,university of cape town,cape town, South Africa, university of malawi college of medicine,blantyre,malawi,liverpool school of tropical medicine,liverpool, United Kingdom, infectious disease,genome institute of singapore, Singapore, brighton and sussex medical school,university of sussex,brighton, United Kingdom, section of paediatrics and wellcome trust centre for clinical tropical medicine,division of infectious diseases,department of medicine,imperial college london,london, United Kingdom, infectious disease,genome institute of singapore, Singapore, division of infectious diseases and hiv medicine,department of medicine,groote schuur hospital,university of cape town,cape town, South Africa, department of infectious diseases,leiden university medical center,leiden, Netherlands, karonga prevention study,chilumba,karonga district, Malawi, section of paediatrics and wellcome trust centre for clinical tropical medicine,division of infectious diseases,department of medicine,imperial college london,london,united kingdom,clinical infectious diseases research initiative,institute of infectious diseases and molecular medicine,university of cape town,cape town,south africa,mrc national institute for medical research,london, United Kingdom, department of genomics of common disease,school of public health,imperial college london,london,united kingdom,institute for molecular bioscience,university of queensland,st lucia,qld, Australia, section of paediatrics and wellcome trust centre for clinical tropical medicine,division of infectious diseases,department of medicine,imperial college london,london, United Kingdom
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Authors
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